BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Scorpion 2

    Reg #: 1313046 · FEI: 1313046 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    20
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    C.R. BARD, INC.
    Registration Number
    1313046
    FEI Number
    1313046
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    289 Bay Rd
    City
    Queensbury
    State
    NY
    ZIP
    12804
    Country
    US

    Owner / Operator

    Firm Name
    C. R. Bard, Inc.
    Operator Number
    2212754
    Address
    1 Becton Drive
    City
    Franklin Lakes
    State
    NJ
    Postal Code
    07417
    Country
    US

    Products

    Device Name Product Code
    Cardiac Ablation Percutaneous Catheter LPB

    Proprietary Names

    Scorpion 2 Over-the-wire Mesh Ablator Cable Kit Tempulsed Pulsed RF Controller IECG Cables HD Mesh Ablator Cables Scorpion 2 M Ablation Catheters Tempulse Pulsed RF Controller Scorpion Stinger SM Over-the-wire Mesh Ablator Diagnostic and Ablation Catheter Bard RF Cardiac Ablation Generator & Associated Cabling Stinger S Scorpion M Ablation Catheter 8mm Distal Tip Electrode Stinger Stinger M Tempulsed Pulsed RF Controller Generator Power Cables HD Mesh Ablator Diagnostic Over-the-Wire Mesh Ablator Guide Wire Tempulsed Pulsed RF Controller Generator Reference Cables Tempulsed Pulsed RF Controller Dual Patient Cables

    Establishment Types

    Manufacture Device in the United States for Export Only